CA2221729A1 - Use of sulfamic acid derivatives, acyl sulfonamides or sulfonyl carbamates for the manufacture of a medicament for lowering lipoprotein levels - Google Patents
Use of sulfamic acid derivatives, acyl sulfonamides or sulfonyl carbamates for the manufacture of a medicament for lowering lipoprotein levels Download PDFInfo
- Publication number
- CA2221729A1 CA2221729A1 CA002221729A CA2221729A CA2221729A1 CA 2221729 A1 CA2221729 A1 CA 2221729A1 CA 002221729 A CA002221729 A CA 002221729A CA 2221729 A CA2221729 A CA 2221729A CA 2221729 A1 CA2221729 A1 CA 2221729A1
- Authority
- CA
- Canada
- Prior art keywords
- methylethyl
- bis
- phenyl
- sulfamic acid
- phenyl ester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- -1 acyl sulfonamides Chemical class 0.000 title claims description 68
- 239000003814 drug Substances 0.000 title description 4
- 102000004895 Lipoproteins Human genes 0.000 title description 3
- 108090001030 Lipoproteins Proteins 0.000 title description 3
- 238000004519 manufacturing process Methods 0.000 title description 3
- 229940124530 sulfonamide Drugs 0.000 title description 3
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 title description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 116
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 74
- 150000001875 compounds Chemical class 0.000 claims abstract description 44
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 33
- 239000001257 hydrogen Substances 0.000 claims abstract description 33
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 27
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 22
- 239000001301 oxygen Substances 0.000 claims abstract description 22
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 10
- 239000011593 sulfur Substances 0.000 claims abstract description 10
- 208000026106 cerebrovascular disease Diseases 0.000 claims abstract description 8
- 208000037803 restenosis Diseases 0.000 claims abstract description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 7
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 7
- 208000018262 Peripheral vascular disease Diseases 0.000 claims abstract description 6
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 70
- 102100040214 Apolipoprotein(a) Human genes 0.000 claims description 44
- 101710115418 Apolipoprotein(a) Proteins 0.000 claims description 36
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 27
- 239000007983 Tris buffer Substances 0.000 claims description 23
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 150000002431 hydrogen Chemical class 0.000 claims description 16
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000000460 chlorine Substances 0.000 claims description 13
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 12
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- HCNHIFFZTIRZJA-UHFFFAOYSA-N [3-[2-(2,6-dichlorophenyl)acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC1=C(Cl)C=CC=C1Cl HCNHIFFZTIRZJA-UHFFFAOYSA-N 0.000 claims description 10
- 125000004423 acyloxy group Chemical group 0.000 claims description 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- SWYZGLWCQFMQJW-UHFFFAOYSA-N phenoxy hypofluorite Chemical compound FOOC1=CC=CC=C1 SWYZGLWCQFMQJW-UHFFFAOYSA-N 0.000 claims description 7
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 5
- SVISWFVZGCSHEK-UHFFFAOYSA-N 2-[2,6-di(propan-2-yl)phenyl]-n-[[2,4,6-tri(propan-2-yl)phenyl]methylsulfonyl]acetamide Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CS(=O)(=O)NC(=O)CC1=C(C(C)C)C=CC=C1C(C)C SVISWFVZGCSHEK-UHFFFAOYSA-N 0.000 claims description 5
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 5
- RPFCHZANSTXMQB-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-(2,2,2-triphenylacetyl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 RPFCHZANSTXMQB-UHFFFAOYSA-N 0.000 claims description 5
- NVCAXWLFXNFPRF-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-(2-thiophen-2-ylacetyl)phenyl] sulfamate Chemical compound S1C(=CC=C1)CC(=O)C=1C(=C(C(=CC1)C(C)C)OS(N)(=O)=O)C(C)C NVCAXWLFXNFPRF-UHFFFAOYSA-N 0.000 claims description 5
- RNYUYZOQGFPICG-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[2-(2,4,6-trimethoxyphenyl)acetyl]phenyl] sulfamate Chemical compound COC1=CC(OC)=CC(OC)=C1CC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C RNYUYZOQGFPICG-UHFFFAOYSA-N 0.000 claims description 5
- LXSBEGRJNHLGJI-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[2-(2,4,6-trimethylphenyl)acetyl]phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC1=C(C)C=C(C)C=C1C LXSBEGRJNHLGJI-UHFFFAOYSA-N 0.000 claims description 5
- FNQIZEQUAUEZSA-UHFFFAOYSA-N [2,6-diphenyl-3-[2-[2,4,6-tri(propan-2-yl)phenyl]acetyl]phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CC(=O)C(C(=C1OS(N)(=O)=O)C=2C=CC=CC=2)=CC=C1C1=CC=CC=C1 FNQIZEQUAUEZSA-UHFFFAOYSA-N 0.000 claims description 5
- IBHZMFUKPWDNEH-UHFFFAOYSA-N [2-[2,4-di(propan-2-yl)-3-sulfamoyloxyphenyl]-2-oxo-1-[2,4,6-tri(propan-2-yl)phenyl]ethyl] acetate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C(OC(C)=O)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C IBHZMFUKPWDNEH-UHFFFAOYSA-N 0.000 claims description 5
- QNRBLGKOBXBNQA-UHFFFAOYSA-N [3-(1-phenylcyclopentanecarbonyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C1(C=2C=CC=CC=2)CCCC1 QNRBLGKOBXBNQA-UHFFFAOYSA-N 0.000 claims description 5
- OWQGQWCZHWFFBB-UHFFFAOYSA-N [3-(2,2-diphenylpropanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C)(C=1C=CC=CC=1)C1=CC=CC=C1 OWQGQWCZHWFFBB-UHFFFAOYSA-N 0.000 claims description 5
- MWMRVLOOUQKYSS-UHFFFAOYSA-N [3-(2-oxo-2-phenylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(=O)C1=CC=CC=C1 MWMRVLOOUQKYSS-UHFFFAOYSA-N 0.000 claims description 5
- LVUYWXXLGSVQEH-UHFFFAOYSA-N [3-(2-phenylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC1=CC=CC=C1 LVUYWXXLGSVQEH-UHFFFAOYSA-N 0.000 claims description 5
- WERGUDHVRRAQIA-UHFFFAOYSA-N [3-(2-phenylbutanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound C=1C=CC=CC=1C(CC)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C WERGUDHVRRAQIA-UHFFFAOYSA-N 0.000 claims description 5
- ONKLECGKWMBEJQ-UHFFFAOYSA-N [3-(2-phenylpropanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C)C1=CC=CC=C1 ONKLECGKWMBEJQ-UHFFFAOYSA-N 0.000 claims description 5
- WUHZAAZJJIQGBP-UHFFFAOYSA-N [3-(3,3-diphenylpropanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC(C=1C=CC=CC=1)C1=CC=CC=C1 WUHZAAZJJIQGBP-UHFFFAOYSA-N 0.000 claims description 5
- BKIZTHMHKWZOPD-UHFFFAOYSA-N [3-(3-methyl-2-phenylpentanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate;sodium Chemical compound [Na].C=1C=CC=CC=1C(C(C)CC)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C BKIZTHMHKWZOPD-UHFFFAOYSA-N 0.000 claims description 5
- IEUKVMHUFHMJNZ-UHFFFAOYSA-N [3-(9h-fluorene-9-carbonyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C1C2=CC=CC=C2C2=CC=CC=C21 IEUKVMHUFHMJNZ-UHFFFAOYSA-N 0.000 claims description 5
- LGCMWWNQMXOKTK-RBUKOAKNSA-N [3-[(1r,2r)-2-phenylcyclopropanecarbonyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)[C@H]1[C@H](C=2C=CC=CC=2)C1 LGCMWWNQMXOKTK-RBUKOAKNSA-N 0.000 claims description 5
- VUKGWEPYJTUIFU-UHFFFAOYSA-N [3-[2-(2,5-dimethoxyphenyl)acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound COC1=CC=C(OC)C(CC(=O)C=2C(=C(OS(N)(=O)=O)C(C(C)C)=CC=2)C(C)C)=C1 VUKGWEPYJTUIFU-UHFFFAOYSA-N 0.000 claims description 5
- XZJUPTJTXXIRGP-UHFFFAOYSA-N [3-[2-[2,6-di(propan-2-yl)phenoxy]acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=CC=CC(C(C)C)=C1OCC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C XZJUPTJTXXIRGP-UHFFFAOYSA-N 0.000 claims description 5
- UVDBZLKUTRQIEF-UHFFFAOYSA-N [3-[2-hydroxy-2-[2,4,6-tri(propan-2-yl)phenyl]acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C(O)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C UVDBZLKUTRQIEF-UHFFFAOYSA-N 0.000 claims description 5
- DXHYZVZSMDLNBQ-UHFFFAOYSA-N [3-decanoyl-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CCCCCCCCCC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C DXHYZVZSMDLNBQ-UHFFFAOYSA-N 0.000 claims description 5
- SDKIUQCUWFKCBF-UHFFFAOYSA-N [3-dodecanoyl-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CCCCCCCCCCCC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C SDKIUQCUWFKCBF-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 230000036470 plasma concentration Effects 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- PZVXVEZHFRHQHE-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[2-[2-(trifluoromethyl)phenyl]acetyl]phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC1=CC=CC=C1C(F)(F)F PZVXVEZHFRHQHE-UHFFFAOYSA-N 0.000 claims description 4
- LPSLDTRJJRBXNB-UHFFFAOYSA-N [2,6-di(propan-2-yl)phenyl]-[[2,4,6-tri(propan-2-yl)phenyl]methylsulfonyl]carbamic acid Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CS(=O)(=O)N(C(O)=O)C1=C(C(C)C)C=CC=C1C(C)C LPSLDTRJJRBXNB-UHFFFAOYSA-N 0.000 claims description 4
- 210000002966 serum Anatomy 0.000 claims description 4
- MLTPEFJUDCICLN-UHFFFAOYSA-M sodium;n-[2,6-di(propan-2-yl)phenyl]-n-[[2,4,6-tri(propan-2-yl)phenyl]methylsulfonyl]carbamate Chemical compound [Na+].CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CS(=O)(=O)N(C([O-])=O)C1=C(C(C)C)C=CC=C1C(C)C MLTPEFJUDCICLN-UHFFFAOYSA-M 0.000 claims description 4
- GRWVKVSNGVJKET-UHFFFAOYSA-N [3-(2-cyclopentyl-2-phenylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C=1C=CC=CC=1)C1CCCC1 GRWVKVSNGVJKET-UHFFFAOYSA-N 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
- 241000124008 Mammalia Species 0.000 claims 5
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 5
- PCVSBMWYSWVMGR-UHFFFAOYSA-N OC1=CC=CC=C1OF Chemical compound OC1=CC=CC=C1OF PCVSBMWYSWVMGR-UHFFFAOYSA-N 0.000 claims 4
- FFHDHZYMGPGQLF-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[2-[2,4,6-tri(propan-2-yl)phenoxy]acetyl]phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1OCC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C FFHDHZYMGPGQLF-UHFFFAOYSA-N 0.000 claims 4
- WQRMTMWIXSZJNP-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[3-[2,4,6-tri(propan-2-yl)phenyl]prop-2-enoyl]phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C=CC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C WQRMTMWIXSZJNP-UHFFFAOYSA-N 0.000 claims 4
- KKSWLSQKFBJGQJ-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-[3-[2,4,6-tri(propan-2-yl)phenyl]propanoyl]phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CCC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C KKSWLSQKFBJGQJ-UHFFFAOYSA-N 0.000 claims 4
- JXIWGHCSLXAJLL-UHFFFAOYSA-N [3-(2,2-diphenylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 JXIWGHCSLXAJLL-UHFFFAOYSA-N 0.000 claims 4
- LHGJDLJINRPFDO-UHFFFAOYSA-N [3-(2-cyclohexyl-2-phenylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)C(C=1C=CC=CC=1)C1CCCCC1 LHGJDLJINRPFDO-UHFFFAOYSA-N 0.000 claims 4
- TVZUKCLORBYVAB-UHFFFAOYSA-N [3-(2-cyclohexylacetyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CC1CCCCC1 TVZUKCLORBYVAB-UHFFFAOYSA-N 0.000 claims 4
- QLCRUODBCQNCBH-UHFFFAOYSA-N [3-(3-methyl-2-phenylpentanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound C=1C=CC=CC=1C(C(C)CC)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C QLCRUODBCQNCBH-UHFFFAOYSA-N 0.000 claims 4
- YKPBDXIXQLCDMW-UHFFFAOYSA-N [3-(3-phenylpropanoyl)-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=C(OS(N)(=O)=O)C(C(C)C)=CC=C1C(=O)CCC1=CC=CC=C1 YKPBDXIXQLCDMW-UHFFFAOYSA-N 0.000 claims 4
- COLDWNCECCAUKF-UHFFFAOYSA-N [3-[2-(1-adamantyl)acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound C12(CC3CC(CC(C1)C3)C2)CC(=O)C=1C(=C(C(=CC=1)C(C)C)OS(N)(=O)=O)C(C)C COLDWNCECCAUKF-UHFFFAOYSA-N 0.000 claims 4
- VWMCJIVWYXESEB-UHFFFAOYSA-N [3-[2-(2-methoxyphenyl)acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound COC1=CC=CC=C1CC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C VWMCJIVWYXESEB-UHFFFAOYSA-N 0.000 claims 4
- ODLHXSJZGOAYGM-UHFFFAOYSA-N [3-[2-[2,6-di(propan-2-yl)phenyl]acetyl]-2,4,6-tri(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=CC=CC(C(C)C)=C1CC(=O)C1=C(C(C)C)C=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C ODLHXSJZGOAYGM-UHFFFAOYSA-N 0.000 claims 4
- XBVKHCGXRZSBCL-UHFFFAOYSA-N [3-[2-[2,6-di(propan-2-yl)phenyl]acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=CC=CC(C(C)C)=C1CC(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C XBVKHCGXRZSBCL-UHFFFAOYSA-N 0.000 claims 4
- DDHOUTXDEJOEFF-UHFFFAOYSA-N [3-[2-fluoro-2-[2,4,6-tri(propan-2-yl)phenyl]acetyl]-2,6-di(propan-2-yl)phenyl] sulfamate Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C(F)C(=O)C1=CC=C(C(C)C)C(OS(N)(=O)=O)=C1C(C)C DDHOUTXDEJOEFF-UHFFFAOYSA-N 0.000 claims 4
- FTUPHZDPMFYSPM-UHFFFAOYSA-N 2-[2,6-di(propan-2-yl)phenyl]-n-[[2,4,6-tri(propan-2-yl)phenyl]methylsulfonyl]acetamide;sodium Chemical compound [Na].CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1CS(=O)(=O)NC(=O)CC1=C(C(C)C)C=CC=C1C(C)C FTUPHZDPMFYSPM-UHFFFAOYSA-N 0.000 claims 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- BOGOAOVZHJYIRZ-UHFFFAOYSA-N [2,6-di(propan-2-yl)-3-(2-thiophen-3-ylacetyl)phenyl] sulfamate Chemical compound S1C=C(C=C1)CC(=O)C=1C(=C(C(=CC1)C(C)C)OS(N)(=O)=O)C(C)C BOGOAOVZHJYIRZ-UHFFFAOYSA-N 0.000 claims 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 2
- BOVHUUQISWANCW-UHFFFAOYSA-M sodium;acetylazanide Chemical compound CC(=O)N[Na] BOVHUUQISWANCW-UHFFFAOYSA-M 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 abstract description 7
- 230000001225 therapeutic effect Effects 0.000 abstract description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 16
- 102000013566 Plasminogen Human genes 0.000 description 10
- 108010051456 Plasminogen Proteins 0.000 description 10
- 102000007330 LDL Lipoproteins Human genes 0.000 description 9
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/325—Carbamic acids; Thiocarbamic acids; Anhydrides or salts thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US303195P | 1995-08-04 | 1995-08-04 | |
| US60/003,031 | 1995-08-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2221729A1 true CA2221729A1 (en) | 1997-02-20 |
Family
ID=21703764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002221729A Abandoned CA2221729A1 (en) | 1995-08-04 | 1996-07-08 | Use of sulfamic acid derivatives, acyl sulfonamides or sulfonyl carbamates for the manufacture of a medicament for lowering lipoprotein levels |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US6117909A (cs) |
| EP (1) | EP0841913B1 (cs) |
| JP (1) | JPH11510184A (cs) |
| KR (1) | KR19990036127A (cs) |
| CN (1) | CN1192140A (cs) |
| AT (1) | ATE232097T1 (cs) |
| AU (1) | AU716255B2 (cs) |
| BG (1) | BG63863B1 (cs) |
| CA (1) | CA2221729A1 (cs) |
| CZ (1) | CZ26198A3 (cs) |
| DE (1) | DE69626118T2 (cs) |
| DK (1) | DK0841913T3 (cs) |
| EA (1) | EA002435B1 (cs) |
| EE (1) | EE9800037A (cs) |
| ES (1) | ES2191762T3 (cs) |
| GE (1) | GEP20012511B (cs) |
| HR (1) | HRP960341A2 (cs) |
| HU (1) | HUP9900668A3 (cs) |
| IL (1) | IL122247A0 (cs) |
| NO (1) | NO980466L (cs) |
| NZ (1) | NZ312571A (cs) |
| PL (1) | PL185943B1 (cs) |
| PT (1) | PT841913E (cs) |
| SK (1) | SK12598A3 (cs) |
| UA (1) | UA46030C2 (cs) |
| WO (1) | WO1997005868A1 (cs) |
| ZA (1) | ZA966617B (cs) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1584333A3 (en) * | 1998-01-28 | 2009-04-29 | Warner-Lambert Company LLC | Use of acetylcoenzime A inhibitors for treating Alzheimer's disease |
| EP1098662A2 (en) * | 1998-07-21 | 2001-05-16 | Warner-Lambert Company | Coadministration of acat and mmp inhibitors for the treatment of atherosclerotic lesions |
| IT1303249B1 (it) * | 1998-10-23 | 2000-11-06 | Dompe Spa | Alcune n-(2-aril-propionil)-solfonammidi e preparazionifarmaceutiche che le contengono. |
| AU1210401A (en) * | 1999-11-05 | 2001-06-06 | Warner-Lambert Company | Prevention of plaque rupture by acat inhibitors |
| CA2369967A1 (en) * | 2001-02-12 | 2002-08-12 | Joseph Anthony Cornicelli | Methods of treating nuclear factor-kappa b mediated diseases and disorders |
| AR037097A1 (es) | 2001-10-05 | 2004-10-20 | Novartis Ag | Compuestos acilsulfonamidas, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento |
| US6939224B2 (en) * | 2002-03-12 | 2005-09-06 | Igt | Gaming device having varying risk player selections |
| US11498904B2 (en) | 2017-11-14 | 2022-11-15 | Merck Sharp & Dohme Llc | Substituted biaryl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors |
| JP7269928B2 (ja) | 2017-11-14 | 2023-05-09 | メルク・シャープ・アンド・ドーム・エルエルシー | インドールアミン ２，３－ジオキシゲナーゼ（ｉｄｏ）阻害剤としての新規の置換ビアリール化合物 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5003106A (en) * | 1983-07-19 | 1991-03-26 | American Cyanamid Company | Antiatherosclerotic ureas and thioureas |
| US5245068A (en) * | 1990-10-30 | 1993-09-14 | Warner-Lambert Company | Oxysulfonyl carbamates |
| ATE116291T1 (de) * | 1990-10-30 | 1995-01-15 | Warner Lambert Co | Oxysulfonylcarbamate. |
| IL101785A0 (en) * | 1991-05-10 | 1992-12-30 | Fujisawa Pharmaceutical Co | Urea derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same |
| IL109431A (en) * | 1993-05-14 | 2001-01-11 | Warner Lambert Co | Pharmaceutical compositions containing n-acyl sulfamic acid esters (or thioesters), n-acyl sulfonamides, and n-sulfonyl carbamic acid esters (or thioesters), for regulating plasma cholesterol concentration, and certain such novel compounds |
| US5491172A (en) * | 1993-05-14 | 1996-02-13 | Warner-Lambert Company | N-acyl sulfamic acid esters (or thioesters), N-acyl sulfonamides, and N-sulfonyl carbamic acid esters (or thioesters) as hypercholesterolemic agents |
-
1996
- 1996-07-08 ES ES96923687T patent/ES2191762T3/es not_active Expired - Lifetime
- 1996-07-08 SK SK125-98A patent/SK12598A3/sk unknown
- 1996-07-08 CA CA002221729A patent/CA2221729A1/en not_active Abandoned
- 1996-07-08 KR KR1019980700795A patent/KR19990036127A/ko not_active Ceased
- 1996-07-08 AT AT96923687T patent/ATE232097T1/de not_active IP Right Cessation
- 1996-07-08 WO PCT/US1996/011366 patent/WO1997005868A1/en not_active Ceased
- 1996-07-08 DE DE69626118T patent/DE69626118T2/de not_active Expired - Fee Related
- 1996-07-08 NZ NZ312571A patent/NZ312571A/en unknown
- 1996-07-08 GE GEAP19964165A patent/GEP20012511B/en unknown
- 1996-07-08 EP EP96923687A patent/EP0841913B1/en not_active Expired - Lifetime
- 1996-07-08 PL PL96324908A patent/PL185943B1/pl unknown
- 1996-07-08 HU HU9900668A patent/HUP9900668A3/hu unknown
- 1996-07-08 CZ CZ98261A patent/CZ26198A3/cs unknown
- 1996-07-08 AU AU64541/96A patent/AU716255B2/en not_active Ceased
- 1996-07-08 US US09/000,296 patent/US6117909A/en not_active Expired - Fee Related
- 1996-07-08 PT PT96923687T patent/PT841913E/pt unknown
- 1996-07-08 EE EE9800037A patent/EE9800037A/xx unknown
- 1996-07-08 JP JP9508427A patent/JPH11510184A/ja active Pending
- 1996-07-08 DK DK96923687T patent/DK0841913T3/da active
- 1996-07-08 EA EA199800176A patent/EA002435B1/ru not_active IP Right Cessation
- 1996-07-08 CN CN96196033A patent/CN1192140A/zh active Pending
- 1996-07-08 IL IL12224796A patent/IL122247A0/xx unknown
- 1996-07-16 HR HR60/003,031A patent/HRP960341A2/hr not_active Application Discontinuation
- 1996-08-02 ZA ZA9606617A patent/ZA966617B/xx unknown
- 1996-08-07 UA UA97126430A patent/UA46030C2/uk unknown
-
1998
- 1998-01-30 BG BG102222A patent/BG63863B1/bg unknown
- 1998-02-03 NO NO980466A patent/NO980466L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69626118T2 (de) | 2003-11-27 |
| HRP960341A2 (en) | 1998-02-28 |
| PL185943B1 (pl) | 2003-09-30 |
| DE69626118D1 (de) | 2003-03-13 |
| JPH11510184A (ja) | 1999-09-07 |
| CZ26198A3 (cs) | 1998-07-15 |
| NO980466D0 (no) | 1998-02-03 |
| ES2191762T3 (es) | 2003-09-16 |
| BG63863B1 (bg) | 2003-04-30 |
| PT841913E (pt) | 2003-06-30 |
| EP0841913A1 (en) | 1998-05-20 |
| DK0841913T3 (da) | 2003-05-05 |
| GEP20012511B (en) | 2001-08-27 |
| CN1192140A (zh) | 1998-09-02 |
| ATE232097T1 (de) | 2003-02-15 |
| AU716255B2 (en) | 2000-02-24 |
| EP0841913B1 (en) | 2003-02-05 |
| HUP9900668A3 (en) | 2000-08-28 |
| EA002435B1 (ru) | 2002-04-25 |
| PL324908A1 (en) | 1998-06-22 |
| NO980466L (no) | 1998-02-03 |
| AU6454196A (en) | 1997-03-05 |
| KR19990036127A (ko) | 1999-05-25 |
| US6117909A (en) | 2000-09-12 |
| HUP9900668A2 (hu) | 1999-06-28 |
| WO1997005868A1 (en) | 1997-02-20 |
| EA199800176A1 (ru) | 1998-10-29 |
| IL122247A0 (en) | 1998-04-05 |
| ZA966617B (en) | 1997-02-18 |
| SK12598A3 (en) | 1999-02-11 |
| NZ312571A (en) | 2000-07-28 |
| BG102222A (en) | 1998-09-30 |
| UA46030C2 (uk) | 2002-05-15 |
| EE9800037A (et) | 1998-08-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |